Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.33 (T)
Location

Chromosome 20:2380344 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs3854714, rs58766410

HGVS name

20:g.2380344T>C

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 2 transcripts, has 3694 sample genotypes and is mentioned in 1 citation.

Variant displays